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Pediatric Clinics of North America
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May 24, 2014
Genetics and ocular disorders: a focused review
Hannah L Scanga, Ken K Nischal
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
February 1, 2020
Reply
Hannah L Scanga, Ken K Nischal
American Journal of Medical Genetics. Part A
|
February 26, 2022
ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent
Hannah L Scanga, Ken K Nischal
Cornea
|
April 12, 2017
Reply
Ken K Nischal, Hannah L Scanga, Jocelyn Kim
American Journal of Medical Genetics. Part A
|
November 12, 2022
Variable phenotype of secondary congenital corneal opacities associated with microphthalmia with linear skin defects syndrome
Elena Franco, Hannah L Scanga, Ken K Nischal
Cornea
|
February 2, 2023
Corneal Plana-Like Phenotype With Peripheral Scleralization Associated With a Pathogenic Variant of PITX2 : A Case Report
Elena Franco, Hannah L Scanga, Ken K Nischal
Ophthalmic Genetics
|
February 19, 2026
Bilateral juvenile-onset cataracts associated with <i>GCNT2</i> variants
Kerollos M Kamel, Hannah L Scanga, Ken K Nischal
Ophthalmic Genetics
|
April 16, 2021
Keratoconus in a child with partial trisomy 13
Julia Ernst, Amgad Eldib, Hannah L Scanga, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
December 3, 2014
Improved visual function with dietary intervention in a child with lipemia retinalis
Valeria Fu, Hannah L Scanga, Anagha Medsinge, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2021
Somatic KRAS mutation affecting codon 146 in linear sebaceous nevus syndrome
Saloni Kapoor, Hannah L Scanga, Miguel Reyes-Múgica, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Pediatric Clinics of North America
|
May 24, 2014
Genetics and ocular disorders: a focused review
Hannah L Scanga, Ken K Nischal
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
February 1, 2020
Reply
Hannah L Scanga, Ken K Nischal
American Journal of Medical Genetics. Part A
|
February 26, 2022
ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent
Hannah L Scanga, Ken K Nischal
Cornea
|
April 12, 2017
Reply
Ken K Nischal, Hannah L Scanga, Jocelyn Kim
American Journal of Medical Genetics. Part A
|
November 12, 2022
Variable phenotype of secondary congenital corneal opacities associated with microphthalmia with linear skin defects syndrome
Elena Franco, Hannah L Scanga, Ken K Nischal
Cornea
|
February 2, 2023
Corneal Plana-Like Phenotype With Peripheral Scleralization Associated With a Pathogenic Variant of PITX2 : A Case Report
Elena Franco, Hannah L Scanga, Ken K Nischal
Ophthalmic Genetics
|
February 19, 2026
Bilateral juvenile-onset cataracts associated with <i>GCNT2</i> variants
Kerollos M Kamel, Hannah L Scanga, Ken K Nischal
Ophthalmic Genetics
|
April 16, 2021
Keratoconus in a child with partial trisomy 13
Julia Ernst, Amgad Eldib, Hannah L Scanga, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
December 3, 2014
Improved visual function with dietary intervention in a child with lipemia retinalis
Valeria Fu, Hannah L Scanga, Anagha Medsinge, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2021
Somatic KRAS mutation affecting codon 146 in linear sebaceous nevus syndrome
Saloni Kapoor, Hannah L Scanga, Miguel Reyes-Múgica, et al.
Page
of 3